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The Navidence Platform 

Driving clear outcomes for your research organization. 

Consistency
A single source of truth across your organization for all operational definitions, code lists and value sets

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Precision
Use CODefs to ensure you data definitions are validated and aligned with scientific, regulatory and industry standards

Efficiency
Remove the need to reinvent the wheel in the generation of data definitions.
 
Streamline code list management.
 
Reduce the time to get from study design to exportable data query from weeks to days

Trust
Use CODefs to support engagement with internal and external stakeholders and show alignment with study design and data source.

 

"We are arguing that there should be a place in our organization where ALL scientific definitions for ALL studies reside. The science in pre-approval and post-approval needs to be consistent and aligned, particularly when linking trial data to real world data."

man-at-design-wall_resize_web
Global VP Epidemiology | Top 10 Pharma
 

Consistency

Align Study Design and Data Science Across Your Organization.

Traditionally Study Design has been performed independently of assessment of Real World Data creating:

  • back and forth across multiple functions.
  • inconsistency in application of study design elements, code lists and value sets.
  • increased risk of multiple iterations of protocol design based on data feasibility.

The Navidence Platform enables researchers to perform study design in a "data query ready" format, allowing faster time to data assessment, and mitigating time and resource across your organization.

Manage the ever-changing landscape of code lists and value sets.

  • Generation and Management of Code Lists and Value Sets is hugely time-consuming for research organisations. The Navidence Platform can provide a resource for the consistent management and application of Code Lists and Value Sets across your organization.

 

"Small differences in the choice of operational definition … may have a large impact on study results.”

FDA-Logo_Web-1
Use of Real-World Evidence to Support Regulatory Decision Making for Medical Devices | December 19, 2023.
 

Precision

A faster and more accurate pathway to "Data Query Ready".

  • Deploy CODef Libraries to your study design and communicate clarity and precision at the study element and data element level.
  • Export your protocol in computable format allowing real world data holders to more accurately assess the suitability for your project.
Communicate fit-for-purpose data assessment to internal and external stakeholders.
  • Regulators and other external stakeholders are increasingly demanding greater levels of precision and transparency in discussions about the potential for use of Real World Data in studies.
  • Export your protocol to show how each study element matches with data souce regulatory decision making.
  • Drive precision for use cases such as Trial Tokenization and External Control Arms.

Speed from Study Design to Data Assessment.

Reduce Time and Costs.

 

  • Research Teams typically spend 8-12 weeks and an average of $77,000 creating and selecting operational definitions, code lists and value sets and ensuring they are aligned with the scientific landscape.

 

  • The Navidence Platform provides ready-to-deploy CODefs that teams can align to their study design reducing costs by an average of 50% and reducing the timeline from Study Design to Data Assessment to a matter of days.
costs

"Our team are spending far less time and resource bridging across the organization. We are dealing with the future rather than reinventing the past."

man-at-design-wall_resize_web
Head Real World Data Science | Top 10 Pharma
 

Efficiency

Have you ever had to ask around your organization to see if anyone else has some code-lists or value sets?

  • See each study designed across your organisation, and which code-lists and value sets were used for each study.
  • Create a study design repository for all your protocols, with the ability to drill down on the operational definitions, code-lists and value sets used to support each one.

"Small differences in the choice of operational definition … may have a large impact on study results.”

FDA-Logo_Web-1
Use of Real-World Evidence to Support Regulatory Decision Making for Medical Devices | December 19, 2023.
 

Trust

Scientific Legitimacy

  • Use CODefs to provide legitimacy in your choice of data definitions is vital for internal and external stakeholders

  • Internal: The Navidence Platform provides research teams with a comprehensive set of data definitions, with supporting scientific literature and validations studies available at the click of a button, and available to your internal stakeholders

  • External: The Navidence Platform has been used to deploy CODefs in high complexity use cases such and Trial Tokenization and External Control arms, with our definitions exported from our platform used to support protocol submission to the FDA.

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Learn more about the Navidence Platform

Deploy CODefs to drive Precision, Consistency, Efficiency and Trust as you move from Study Design to Data Assessment

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